Variant #0000953646 (NC_000019.9:g.13002678T>C, NM_000159.3:c.161T>C (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Effect unknown
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.13002678T>C
DNA change (hg38) g.12891864T>C
Published as -
ISCN -
DB-ID GCDH_000279 See all 2 reported entries
Variant remarks ACMG/ACGS: PM3_Supporting, PP3_Moderate, PS3_Supporting, PM2_Supporting (December 2023)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Sabrina Oeser
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Sabrina Oeser
Date created 2023-12-15 16:06:43 +01:00 (CET)
Date last edited 2024-11-11 13:49:39 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +?/? 4 c.161T>C r.(?) p.(Leu54Pro)


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